Canonical Allele Identifier: CA2515993610
Gene: LINC00951 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40353984G>T , CM000668.2:g.40353984G>T GRCh38
NC_000006.11:g.40321723G>T , CM000668.1:g.40321723G>T GRCh37
NC_000006.10:g.40429701G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.2023C>A